Dynamic Q Angle and Core Endurance in Adolescent Athletes With Patellofemoral Pain Syndrome
PFPS-QCORE
Dynamic Q Angle And Core Endurance In Adolescent Athletes With Patellofemoral Pain Syndrome: A Sex-Based Comparative Study
1 other identifier
observational
150
1 country
1
Brief Summary
This observational, cross-sectional study aimed to compare dynamic Q-angle, trunk/core endurance, and lower-extremity flexibility between elite adolescent female and male sprinters with and without patellofemoral pain syndrome (PFPS). Participants were classified according to sex and PFPS status. Dynamic Q-angle was assessed during a standardized step-down task, trunk endurance was evaluated using McGill flexion, extension, and lateral endurance tests, and lower-extremity flexibility was assessed using the Straight Leg Raise, Modified Thomas, and Ober tests. The study also examined whether sex and PFPS status were independently associated with dynamic Q-angle. No therapeutic or experimental intervention was administered.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Dec 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2025
CompletedFirst Submitted
Initial submission to the registry
December 26, 2025
CompletedFirst Posted
Study publicly available on registry
January 9, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
February 20, 2026
CompletedJuly 20, 2026
July 1, 2026
3 months
December 26, 2025
July 16, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Dynamic Q-Angle During the Step-Down Test (degrees)
Dynamic Q-angle was assessed during a standardized step-down task from a 16-cm platform using the DrGoniometer mobile application. Anatomical markers were placed over the anterior superior iliac spine, center of the patella, and tibial tuberosity. Two repetitions were recorded in the frontal plane, and the mean angle was used for analysis. In participants with PFPS, the symptomatic extremity was assessed; in participants without PFPS, the corresponding matched extremity was used.
Baseline (single assessment at study enrollment)
Secondary Outcomes (4)
Trunk/Core Endurance Test Duration (seconds)
Baseline (single assessment at study enrollment)
Hamstring Flexibility - Straight Leg Raise Angle (degrees)
Baseline (single assessment at study enrollment)
Hip Flexor Flexibility - Modified Thomas Test Angle (degrees)
Baseline (single assessment at study enrollment)
Iliotibial Band and Tensor Fasciae Latae Flexibility - Ober Test Angle (degrees)
Baseline (single assessment at study enrollment)
Study Arms (4)
Female Sprinters Without PFPS
Elite adolescent female sprinters aged 15-17 years without current anterior knee pain or clinical findings consistent with patellofemoral pain syndrome. Participants underwent a single standardized assessment of dynamic Q-angle, trunk/core endurance, and lower-extremity flexibility. No therapeutic or experimental intervention was administered.
Female Sprinters With PFPS
Elite adolescent female sprinters aged 15-17 years diagnosed with patellofemoral pain syndrome by a sports medicine physician. Participants underwent a single standardized assessment of dynamic Q-angle, trunk/core endurance, and lower-extremity flexibility. No therapeutic or experimental intervention was administered.
Male Sprinters Without PFPS
Elite adolescent male sprinters aged 15-17 years without current anterior knee pain or clinical findings consistent with patellofemoral pain syndrome. Participants underwent a single standardized assessment of dynamic Q-angle, trunk/core endurance, and lower-extremity flexibility. No therapeutic or experimental intervention was administered.
Male Sprinters With PFPS
Elite adolescent male sprinters aged 15-17 years diagnosed with patellofemoral pain syndrome by a sports medicine physician. Participants underwent a single standardized assessment of dynamic Q-angle, trunk/core endurance, and lower-extremity flexibility. No therapeutic or experimental intervention was administered.
Interventions
Participants were classified as having patellofemoral pain syndrome (PFPS) or not having PFPS based on a clinical assessment performed by a sports medicine physician. PFPS classification was based on anterior knee pain symptoms, positive patellofemoral clinical tests, an Anterior Knee Pain Scale score below 80, and a Visual Analog Scale pain score of at least 3. Biological sex was used as an additional grouping factor. No therapeutic, exercise, pharmacological, or experimental intervention was administered.
Eligibility Criteria
Elite female and male adolescent sprinters aged 15-17 years who were actively competing in national or international sprint events. Participants were evaluated at the Physiotherapy and Rehabilitation Clinic of the Adana Olympic Preparation Center, Provincial Directorate of Youth and Sports, Adana, Türkiye. Participants were classified according to biological sex and the presence or absence of patellofemoral pain syndrome.
You may qualify if:
- Female or male adolescent elite sprinters aged 15-17 years Minimum of two years of regular athletic training Participation in athletic training at least four days per week Possession of a valid track and field license Active participation in sprint events at the national or international level Ability to complete all clinical and biomechanical assessments Written informed consent from the participant and a parent or legal guardian
- PFPS Group-Specific Criteria:
- Diagnosis of patellofemoral pain syndrome by a sports medicine physician Anterior knee pain localized to the patellofemoral region Positive patellar compression and grind test Anterior Knee Pain Scale score below 80 Visual Analog Scale pain score of at least 3
- Control Group-Specific Criteria:
- No current anterior knee pain No clinical findings consistent with patellofemoral pain syndrome
You may not qualify if:
- History of lower-extremity surgery Acute lower-extremity injury within the previous six months Notable musculoskeletal deformity Arthritis or chronic pain affecting the knee, hip, or ankle Neurological or systemic disease that could affect movement or physical performance Inability to complete the assessments because of excessive pain or insufficient cooperation Incomplete assessment data
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Burcin Ugur Tosun
Adana, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
burcin ugur tosun
Ministry of Youth and Sports, Olympic Preparation Center, Adana, Türkiye
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator PhD Physiotherapist Burcin Ugur Tosun
Study Record Dates
First Submitted
December 26, 2025
First Posted
January 9, 2026
Study Start
December 1, 2025
Primary Completion
February 15, 2026
Study Completion
February 20, 2026
Last Updated
July 20, 2026
Record last verified: 2026-07